Halofluorination of alkenes using tetrabutylammonium dihydrogentrifluoride

Manabu Kuroboshi, Tamejiro Hiyama

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

Regio-, stereo-, and chemoselective halofluorination of alkenes is achieved using N-haloamides and tetrabutylammonium dihydrogentrifluoride, and the resulting F-I adducts were successfully converted into fluoroalkenes under dehydroiodination with 1,8-diazabicyclo[5.4.0]undec-7-ene.

Original languageEnglish
Pages (from-to)1215-1218
Number of pages4
JournalTetrahedron Letters
Volume32
Issue number9
DOIs
Publication statusPublished - Feb 25 1991
Externally publishedYes

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Alkenes
tetrabutylammonium
1,8-diazabicyclo(5.4.0)undec-7-ene

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Halofluorination of alkenes using tetrabutylammonium dihydrogentrifluoride. / Kuroboshi, Manabu; Hiyama, Tamejiro.

In: Tetrahedron Letters, Vol. 32, No. 9, 25.02.1991, p. 1215-1218.

Research output: Contribution to journalArticle

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